US4687789A - Water soluble dispersant for water-based pigment compounds comprising a terpolymer of acrylic acid methacrylic acid and itaconic acid - Google Patents
Water soluble dispersant for water-based pigment compounds comprising a terpolymer of acrylic acid methacrylic acid and itaconic acid Download PDFInfo
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- US4687789A US4687789A US06/837,575 US83757586A US4687789A US 4687789 A US4687789 A US 4687789A US 83757586 A US83757586 A US 83757586A US 4687789 A US4687789 A US 4687789A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/04—Anhydrides, e.g. cyclic anhydrides
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/45—Anti-settling agents
Definitions
- the subject of this invention is a water soluble dispersant for water-based pigment compounds, formed from acrylic, methacrylic and itaconic acid copolymers.
- This invention also concerns water-based pigment compounds prepared with this type of dispersant.
- Water-based pigment compounds are known to specialists which consist of a liquid phase, which may be water or an organic solvent which can be mixed with water, or even of a mixture of the two, of a so-called “emulsion polymer” in the liquid phase, also known as the "binder” and of pigments and fillers which may be either totally or partially inert or reactive with their surrounding medium, such as zinc oxide, for example; such compounds may also contain various additives such as biocides, thickeners and anti-foaming agents and so on, and finally a pigment and filler dispersant consisting of a polymer which is water soluble, unlike the "binder” which consists of the emulsion polymer.
- the emulsion polymer is prepared by the copolymerization of monomers such as vinyl acetate and butyl acrylate, for example, in the presence of a protective colloid such as hydroxyethyl cellulose, for example, which is added to the compound in the course of polymerization.
- a protective colloid such as hydroxyethyl cellulose, for example, which is added to the compound in the course of polymerization.
- the emulsion polymer which contains a considerable density of anionic groups, is produced by copolymerization in the absence of protective colloids, of hydrophobic monomers such as styrene and butyl acrylate, for example, and from an anionic hydrophilic monomer such as acrylic acid, for example.
- hydrophobic monomers such as styrene and butyl acrylate, for example
- anionic hydrophilic monomer such as acrylic acid
- carboxylic groups which are present at the surface of particles of emulsion polymers exert a stabilizing effect
- these same carboxylic groups are also capable of reacting with the soluable fraction of the reactive pigment and of thus creating a bond between the particles of the emulsion.
- the metallic ion of the partially soluble reactive pigment creates bonds between the particles of the emulsion polymer.
- this reaction within the water-based pigment compounds between the partially soluble reactive pigment and the emulsion polymer brings about a rise in the viscosity of the compound concerned, which may even result in its solidification.
- This dispersant is a copolymer of an unsaturated mono-carboxylic acid with 40-95 mole percent, such as acrylic, methacrylic or crotonic acid together with the ester of an unsaturated carboxylic acid with 5-60 mole percent such as methyl, ethyl, propyl or butyl acrylate, methyl methacrylate and ethyl crotonate.
- This copolymer is employed as a dispersant in emulsion paints containing non-reactive inorganic pigments and a binder, the average molecular weight of such a copolymer being below 75,000.
- a further type of water soluble pigment dispersant is claimed in UK Pat. No. 985,276 for the creation of stable, water-based suspensions of pigments or organic or inorganic origin.
- This dispersant is a copolymer of acrylic acid, methacrylic acid or of one or several mono or polyalcohol esters of aliphatic chains above 12 carbon atoms, of acrylic and/or methacrylic acids.
- Water soluble additives of this type are recognized to possess excellent dispersive properties for the preparation of water-based pigment compounds such as water-based emulsion coatings, this is because of their pigment dispersing activity and their ability to stabilize the medium over longer periods during which the pigments employed remain inert with regard to the medium, that is to say whenever such pigments as titanium dioxide or other derivatives of titanium, barium sulfate, calcium carbonate, silica, talc, mica, various clays, iron oxide, carbon black or cadmium sulfide are employed, for example and remain inert with regard to the emulsion polymer (binder).
- pigments as titanium dioxide or other derivatives of titanium, barium sulfate, calcium carbonate, silica, talc, mica, various clays, iron oxide, carbon black or cadmium sulfide are employed, for example and remain inert with regard to the emulsion polymer (binder).
- water-based pigment compounds contain at least one reactive pigment with a tendency to dissolve under the conditions under which it is processed; typical pigments of this kind include zinc oxide, lead silico-chromate, zinc chromate, barium metaborate or zinc molybdate, all which are commonly employed in the manufacture of corrosion-resistant paints.
- typical pigments of this kind include zinc oxide, lead silico-chromate, zinc chromate, barium metaborate or zinc molybdate, all which are commonly employed in the manufacture of corrosion-resistant paints.
- all of these reactive pigments display incompatibility with regard to polymer emulsions of the second type (binders). This shows itself by an often frequent and always deleterious and irreversible rise in the viscosity of the water-based pigment compounds which thus become unfit for their intended purpose, some of them even solidifying in the process.
- the effectiveness of the copolymer which it is claimed in the French patent application referred to above, acts as a dispersant, will vary very greatly depending on whether the emulsion copolymer or binder concerned is of the type with or without protective colloids (first or second types, respectively).
- the above-mentioned water-based compounds that is to say compounds containing at least one reactive pigment prepared in the presence of one of the dispersants referred to in the above-mentioned French patent, provide results which are perfectly acceptable to the expert and which are entirely comparable to those obtained with water-based pigment compounds using non-reactive pigments. In other words, there is no alteration in the rheological characteristics of pigments of water-based compounds of this type over a period of time.
- the water soluble dispersant according to this invention which is an acrylic copolymer, is typically a copolymer of acrylic, methacrylic and itaconic acids.
- Copolymers according to this invention generally contain 2.5-96% by weight but preferably 5-70% by weight of acrylic acid, from 2-85% but preferably 5-70% of methacrylic acid and 2-40% but preferably 5-35% of itaconic acid.
- the water soluble pigment dispersant is a copolymer of at least one ethylenic acid and of at least one ethylenic ester
- the water soluble dispersant is a copolymer which entirely consists of three ethylenic acids.
- acrylic copolymers are prepared according to known processes by radical copolymerization of acrylic, methacrylic and itaconic acids in the presence of either a redox polymerization system using typically organic compounds based on hydroxylamine, metabisulfite, peroxides and persalts, for example, such as hydrogen peroxide or persulfate . . . , either in the presence of initiators such as azobisdi-isobutyronitrile, whether in the presence or not of chain transfer agents such as alcohols or mercaptans . . . .
- the aqueous polymerisate solution obtained can be used as it is as an acid or can be partially or totally neutralized by at least one suitable neutralizing agent with a mono or polyvalent function.
- the total or partial neutralizing agent with a monovalent function is selected from a group consisting of alkaline cations, in particular sodium and potassium, or possibly ammonium or even primary, secondary or teritary aliphatic and/or cyclical amines, such as the ethanol amines (mono, di- or tri-ethanol amine), mono and di-ethylamine, cyclohexylamine, methyl-cyclohexylamine or amino-methylpropanol . . . .
- the partial or total neutralizing agent with a polyvalent function is on the other hand selected from a group consisting of divalent alkaline earth cations, in particular magnesium, manganese and calcium or even zinc, and also by trivalent cations, aluminum or even in the case of cations of higher valency such as aliphatic and/or cyclical polyamines such as ethylene diamine, diethylene triamine and phenylene diamine, for example.
- the partial or toal neutralization of the acid copolymer sites can be easily obtained by the possible combinations between at least one neutralizing agent with a monovalent function and at least one neutralizing agent with a polyvalent function.
- the aqueous polymerisate solution can also be processed by all state-of-the-art methods to eliminate its liquid phase and isolate the acrylic copolymers in the form of a fine powder which can be used in this other form as a dispersant.
- the water soluble dispersant according to this invention is, as the applicants have been able to establish, a fraction of acrylic, methacrylic and itaconic acid copolymers whose specific viscosity lies in the range of 0.3-1.6, and preferably between 0.4-1.0.
- a copolymer solution is prepared in the form of a sodium salt by dissolving 50 g of dry copolymer in 1,000 ml of a solution made of distilled water and 60 g of sodium chloride. Then, with a capillary viscosimeter placed in a bath thermostatically controlled at 25° C., one measures the time taken for a given volume of the above solution containing the alkaline acrylic copolymer to run off and also the time taken for the same volume of the aqueous sodium chloride solution without the above copolymers.
- Specific viscosity " ⁇ " can now be defined according to the following relation: ##EQU1##
- the capillary tube is usually selected so that the flow time of the NaCl solution without the copolymer is about 90-100 seconds, thus providing a very highly accurate measurement of specific viscosity.
- This invention also concerns water-based pigment compounds comprising a liquid phase, an emulsion polymer of the second type obtained by copolymerization of hydrophobic monomers and of an anionic hydrophilic monomer, of finely powdered pigments, one of which at least is reactive with regard to its own medium, inorganic fillers, various state-of-the-art additives and finally the dispersant which is a water soluble copolymer of the type defined in the framework of this invention.
- the pigments used in the preparation of water-based pigment compounds according to this invention are generally polyvalent metal compounds of which typical examples are non-reactive pigments such as titanium dioxide as well as the other pigments derived from titanium, barium sulfate, calcium carbonate, kaolin, talc, mica, silica, clays in general, ferrous oxide, carbon black, cadmium sulfide, chrome oxides but also pigments which are reactive with their medium, such as typically and preferably zinc oxide, zinc molybdate, zinc chromate, lead silico-chromate, barium metaborate, and titanium oxides surface-treated with a coating containing zinc oxide.
- non-reactive pigments such as titanium dioxide as well as the other pigments derived from titanium, barium sulfate, calcium carbonate, kaolin, talc, mica, silica, clays in general, ferrous oxide, carbon black, cadmium sulfide, chrome oxides
- pigments which are reactive with their medium such as typically and preferably zinc
- Water-based pigment compounds according to this invention compared with those using prior art dispersants can be handled even when they have a high dry matter content, that is to say a low liquid phase, as well as other lengthy periods at rest, even after several months.
- the liquid phase of this type of compound generally consists of water and/or a compound which can be mixed with water such as a mono or polyalcohol, for example a mono and polyglycol, ethers and esters of mono or polyalcohol or of mono or polyglycol, such as for example, ethylene glycol, diethylene glycol or propylene glycol.
- a mono or polyalcohol for example a mono and polyglycol, ethers and esters of mono or polyalcohol or of mono or polyglycol, such as for example, ethylene glycol, diethylene glycol or propylene glycol.
- the water soluble pigment dispersant is introduced into the water-based pigment compounds in proportions of 0.05-10, and preferably 0.5-5, which proportions are expressed in terms of a percentage by weight compared with the weight of pigments and fillers.
- water-based pigment compounds according to this invention may also contain, in line with known practice, other components than the pigment, dispersant and the dispersive liquid phase, which components are added to achieve specific effects.
- possible additives include biocides, anionic or non-ionic surfactants of the well-known type.
- anti-foaming agents such as alcohols, mineral oils and silane compounds may also be added at the same time to water-based pigment compounds.
- thickeners can be used in water-based pigment compounds in order to modify their rheological characteristics with the aim of improving the smoothness of the film on the base, for example or to improve the stability of the pigment suspension.
- Thickeners of the well-known type which are used traditionally include for example methyl cellulose, hydroxyethyl cellulose, polyacrylic acid, acrylic and methacrylic copolymers as well as thickeners of the water soluble polyurethane-type which confer improved rheological properties on water-based pigment compounds.
- coalescing agents can also be added to water-based pigment compounds, which may consist of an organic solvent which may or may not mix with water such as, for example, ether-monobutylic ethylene glycol or even 2.2.4-trimethylpentanediol-1.3 mono-isobutyrate (Texanol manufactured by Eastman Chemical Products).
- water-based pigment compounds can be produced in the following known way (or in any known way) which consists of preparing under constant stirring a water-based solution of the dispersant copolymer according to this invention, to which the pigment(s) have been added.
- the medium which is obtained in this way to which various additives of the types already referred to can be added (such as surfactants, thickeners, anti-foaming agents, biocides and coalescents) can undergo a grinding process using traditional techniques such as high speed dissolvers or micro-element grinders.
- additives of the types already referred to such as surfactants, thickeners, anti-foaming agents, biocides and coalescents
- the amount of water soluble pigment dispersant to be employed will be selected within the range defined above. However, as any expert knows, this quantity will depend on the size, shape and type of the particles concerned.
- the familiar method of demonstrating the excellent dispersive characteristics of copolymers according to this invention and especially their ability to be employed in water-based pigment compounds where the pigments are partially or entirely reactive consists of using zinc oxide as the reactive pigment since this substance generally causes real stability problems when it is used in compounds together with an emulsion polymer of the second type as a binder.
- paint prepared with this reactive pigment dispersed by means of one of the previously known substances will display poor stability characteristics over periods of time.
- zinc oxide will partially dissolve and react with the emulsion polymer (binder) and will cause rapid degradation of the rheological characteristics of such a paint, despite the presence of a dispersant.
- a paint prepared with the same reactive pigment using a dispersant according to the invention and where an emulsion polymer of the second type is employed displays excellent stability over periods of time since the effectiveness of this substance can be demonstrated by the fact that the print will maintain its viscosity even after six months' aging at ambient temperature and/or one month at 60° C.
- the principal property of the dispersant according to this invention lies in the fact that when it is employed in water-based pigment compounds, no sharp rise in viscosity is observed, nor does the product solidify during lengthy storage at ambient temperatures or during shorter term exposure to higher temperatures, when a reactive type of pigment is used.
- This example illustrates the use of some typical earlier state-of-the-art water-based pigment compounds, comprising among other constituents zinc oxide as a reactive pigment, an emulsion polymer or binder belonging to both of the categories referred to above and the sodium salt of a homopolymer of methacrylic acid which is a dispersant of a type formerly in common use.
- paint was prepared according to the following method: the following constituents, expressed in parts by weight, were added one after another in a suitable two liter container, fitted with a so-called “shear-type turbine” stirring device rotating at about 1,000 rpm (this is a Cowles-type dissolver with which specialists are familiar):
- This example shows three typical water-based pigment compounds according to earlier state-of-the-art, comprising among their various constituents zinc oxide as a reactive pigment, an emulsion polymer (binder) belonging to the type 2 classification referred to above without protective colloids, and various dispersants used in earlier state-of-the-art techniques.
- a semigloss paint was prepared according to the same method as used in Example 1 above, by adding the following components in turn, the quantities being expressed in parts by weight:
- This example shows a means of preparing the dispersant according to this invention.
- a 1,000 ml vessel was fitted with a mechanical stirrer, a vertical condensor, a means of heating and three dosing pumps.
- Solutions 2 and 3 comprise the redox polymerization system.
- Example 3 illustrates the preparation, according to the method described in Example 3, of dispersants based either on earlier state-of-the-art or according to this invention, and other incorporation in water-based pigment compounds comprising among their various constituents zinc oxide as a reactive pigment, a type 2 emulsion polymer (or binder) referred to above, that is to say without protective colloids and various dispersants from earlier state-of-the-art practice (formulations 7-10) as well as dispersants according to this invention (formulations 11-16).
- Example 3 For the preparation of dispersants, both of the earlier state-of-the-art type as well as according to this invention, the three water-based solutions referred to in Example 3 were used, the first solution containing monomers and solutions 2 and 3 constituting the redox polymerization system.
- a paint was then prepared (a water-based pigment compound) according to the same method as Example 1, by adding in turn the following constituents expressed in parts by weight:
- the water soluble dispersant according to this invention is a fraction of acrylic, methacrylic and itaconic acid copolymers whose specific viscosity is selected between 0.3-1.6 and preferably between 0.4-1.0.
- dispersants according to this invention were prepared using the method described in Example 3, varying the quantity of the redox system employed.
- the dispersant according to the invention very rapidly loses its effectiveness, as shown by the viscosity changes affecting water-based pigment compounds containing these dispersants.
- the purpose of this example is to verify that the dispersant according to this invention must be a copolymer formed from three acrylic, methacrylic and itaconic acid monomers and that copolymerization of these monomers pair by pair results in dispersants whose effectiveness is reduced when they are incorporated in water-based pigment compounds containing a reactive pigment such as zinc oxide and an emulsion polymer (type 2) without a protective colloid.
- a reactive pigment such as zinc oxide and an emulsion polymer (type 2) without a protective colloid.
- dispersants obtained by copolymerization of two monomers selected among the three referred to above were prepared according to the method used in Example 3 (refs. O, P and Q).
- the dispersant according to this invention be an acrylic, methacrylic and itaconic acid copolymer.
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Abstract
A water soluble ethylenic copolymer-based dispersant for water-based pigment compounds, comprising a liquid phase, a binder which is an emulsion polymer, especially without protective colloids and which contains a considerable density of anionic groups, of pigments wholly or partially reactive with regard to their medium by the creation of bonds between the particles of emulsion polymer and the metallic ion of the partially soluble reactive pigment, characterized by the fact that in order to confer on such water-based pigment compounds definable rheological characteristics, which can be adjusted in advance and remain stable over periods of time, the said water soluble dispersant is an acrylic, methacrylic and itaconic acid copolymer.
Description
This application is a continuation of application Ser. No. 739,704, filed May 31, 1985, now abandoned.
The subject of this invention is a water soluble dispersant for water-based pigment compounds, formed from acrylic, methacrylic and itaconic acid copolymers.
This invention also concerns water-based pigment compounds prepared with this type of dispersant.
Water-based pigment compounds are known to specialists which consist of a liquid phase, which may be water or an organic solvent which can be mixed with water, or even of a mixture of the two, of a so-called "emulsion polymer" in the liquid phase, also known as the "binder" and of pigments and fillers which may be either totally or partially inert or reactive with their surrounding medium, such as zinc oxide, for example; such compounds may also contain various additives such as biocides, thickeners and anti-foaming agents and so on, and finally a pigment and filler dispersant consisting of a polymer which is water soluble, unlike the "binder" which consists of the emulsion polymer.
It has been known for some while that in practice the simultaneous presence in a water-based pigment compound of certain emulsion polymers together with a reactive pigment such as zinc oxide, lead silico-chromate, zinc chromate, even when the latter accounts for only a very small proportion of the pigments present in the medium, brings about a change in the rheological characteristics of the compound concerned, which manifests itself by an often rapid and always irreversible rise in viscosity, which may even lead to gelification or solidification in extreme cases.
Two types of state-of-the-art emulsion polymer are known, which have been used in the past as pigment binders in water-based pigment compounds.
In the first instance, the emulsion polymer is prepared by the copolymerization of monomers such as vinyl acetate and butyl acrylate, for example, in the presence of a protective colloid such as hydroxyethyl cellulose, for example, which is added to the compound in the course of polymerization. The use of this first type of emulsion polymer as a binder in water-based pigment compounds, while reactive pigments are present, does not generally change the rheological characteristics of these compounds.
In the second instance which is very much more widely used than the first, the emulsion polymer, which contains a considerable density of anionic groups, is produced by copolymerization in the absence of protective colloids, of hydrophobic monomers such as styrene and butyl acrylate, for example, and from an anionic hydrophilic monomer such as acrylic acid, for example. The use of this second type of emulsion polymer as a binder in water-based pigment compounds causes changes in their rheological characteristics. Although the carboxylic groups which are present at the surface of particles of emulsion polymers exert a stabilizing effect, these same carboxylic groups are also capable of reacting with the soluable fraction of the reactive pigment and of thus creating a bond between the particles of the emulsion. In other words, the metallic ion of the partially soluble reactive pigment creates bonds between the particles of the emulsion polymer. As a result, this reaction within the water-based pigment compounds between the partially soluble reactive pigment and the emulsion polymer brings about a rise in the viscosity of the compound concerned, which may even result in its solidification.
Between these two extreme cases of emulsion polymer, there are also instances of emulsion polymers which are hybrids of the two types referred to here.
It can thus be seen that rheological characteristics of water-based pigment compounds of this type can be significantly modified as a result of the simultaneous presence of an emulsion polymer of the second type and of an even only slightly soluble reactive pigment.
Thus, the deleterious effect of this second type of emulsion polymer on reactive pigments as well as the ever more widespread use of emulsion polymers of the second type in water-based pigment compounds for coating purposes in particular, have been the two reasons which have stimulated specialists to add a water soluble dispersant to water-based pigment compounds of this type, especially in cases where one of the pigments present is reactive with its own medium. The presence of a dispersant of this type can be expected to help deflocculation of the elementary particles and to maintain deflocculation at an optimal level since the fineness of the pigment does not merely enhance its covering power but also improves the opacity and appearance of a coating produced in this way. In other words, the presence of a pigment dispersant is desirable in order to combat the natural tendency of pigments to form aggregates in water-based emulsions, which contribute to decreasing covering power and lead to modification of rheological characteristics.
Numerous dispersants have already been put forward to specialists for use in water-based pigment compounds and have been widely described in the technical literature:
The first type of dispersant to be put forward was proposed in Canadian patent No. 655,884 which consisted of a copolymer of methacrylic acid and acrylic and methacrylic esters using an excess persulfate as initiator of polymerization, since the sulfate groups present in the copolymer are reputed to be responsible for the excellent pigment dispersing properties of the copolymer produced in this way.
An other type of water soluble pigment dispersant is described in U.S. Pat. No. 3,840,487. This dispersant is a copolymer of an unsaturated mono-carboxylic acid with 40-95 mole percent, such as acrylic, methacrylic or crotonic acid together with the ester of an unsaturated carboxylic acid with 5-60 mole percent such as methyl, ethyl, propyl or butyl acrylate, methyl methacrylate and ethyl crotonate. This copolymer is employed as a dispersant in emulsion paints containing non-reactive inorganic pigments and a binder, the average molecular weight of such a copolymer being below 75,000.
A further type of water soluble pigment dispersant is claimed in UK Pat. No. 985,276 for the creation of stable, water-based suspensions of pigments or organic or inorganic origin. This dispersant is a copolymer of acrylic acid, methacrylic acid or of one or several mono or polyalcohol esters of aliphatic chains above 12 carbon atoms, of acrylic and/or methacrylic acids.
In addition to the above, an other type of water soluble pigment dispersant is also described in U.S. Pat. No. 3,980,602. This dispersant, which is an acrylic copolymer with an average molecular weight of 500-30,000, consisting of:
(a) 20-80% by weight of a constituent selected from a group comprising styrene, an alkyl methacrylate or a mixture of styrene and alkyl methacrylate,
(b) 15-55% by weight of an alkyl acrylate, where the alkyl group contains 2-12 carbon atoms,
(c) Finally, 3-25% by weight of acrylic or methacrylic acid.
Then, there is an other type of water soluble pigment dispersant which is described in U.S. Pat. No. 2,930,775 and consists of a copolymer of maleic anhydride and di-isobutylene of a molecular weight between 750-5,000. Water soluble additives of this type are recognized to possess excellent dispersive properties for the preparation of water-based pigment compounds such as water-based emulsion coatings, this is because of their pigment dispersing activity and their ability to stabilize the medium over longer periods during which the pigments employed remain inert with regard to the medium, that is to say whenever such pigments as titanium dioxide or other derivatives of titanium, barium sulfate, calcium carbonate, silica, talc, mica, various clays, iron oxide, carbon black or cadmium sulfide are employed, for example and remain inert with regard to the emulsion polymer (binder).
However, the situation is quite different when water-based pigment compounds contain at least one reactive pigment with a tendency to dissolve under the conditions under which it is processed; typical pigments of this kind include zinc oxide, lead silico-chromate, zinc chromate, barium metaborate or zinc molybdate, all which are commonly employed in the manufacture of corrosion-resistant paints. As has been stated above, all of these reactive pigments display incompatibility with regard to polymer emulsions of the second type (binders). This shows itself by an often frequent and always deleterious and irreversible rise in the viscosity of the water-based pigment compounds which thus become unfit for their intended purpose, some of them even solidifying in the process.
An attempt to eliminate the above disadvantages which result from incompatibility between certain reactive pigments and the emulsion polymers commonly employed in the preparation of water-based pigment compounds, can be found in a proposal contained in the French technical literature (French Pat. No. 2 404 017) to employ a water soluble dispersant comprising an ethylenic copolymer with the following composition:
(a) Over 25% by weight of motives of one or several alpha-, beta monoethylenically unsaturated carboxylic acids as a salt or free acid such as acrylic and methacrylic acids, other alpha-substituted polymerizable acrylic acids or itaconic acid, whereby methacrylic and acrylic acids are preferred.
(b) Motives of at least one other ethylenically unsaturated monomer selected from the group comprising acrylic and methacrylic esters of aliphatic, cycloaliphatic or aromatic C1 -C18 alcohols, styrene, acrylonitrile or vinyl acetate . . . where the average molecular weight of the copolymer constituting the dispersant lies between 500 and 15,000.
Now, as the applicant has had numerous occasions to observe during the experimental preparation of water-based pigment compounds where at least one of the pigments is reactive, such as zinc oxide, the effectiveness of the copolymer, which it is claimed in the French patent application referred to above, acts as a dispersant, will vary very greatly depending on whether the emulsion copolymer or binder concerned is of the type with or without protective colloids (first or second types, respectively). In cases where the emulsion polymer is accompanied by protective colloids, the above-mentioned water-based compounds, that is to say compounds containing at least one reactive pigment prepared in the presence of one of the dispersants referred to in the above-mentioned French patent, provide results which are perfectly acceptable to the expert and which are entirely comparable to those obtained with water-based pigment compounds using non-reactive pigments. In other words, there is no alteration in the rheological characteristics of pigments of water-based compounds of this type over a period of time.
On the other hand, in cases where the emulsion polymer or binder is not accompanied by protective colloids (second type), water-based compounds containing at least one reactive pigment and prepared in the presence of at least one of the dispersants referred to in the above-mentioned French patent, display considerable anomalies which manifest themselves by a rapid and irreversible deterioration of their rheological characteristics, thus displaying an incompatibility between reactive pigments on the one hand and the emulsion polymer on the other. This incompatibility which is highly unacceptable to the specialist, reveals itself, for example, by a considerable rise in the viscosity over a period of time, since the metallic ion of the partially soluble reactive pigment creates a bond between the particles of the emulsion polymer which, as has been said above, is the cause of the observed rise in the viscosity.
Given the economic and technical requirements for water-based pigment compounds of well defined rheological characteristics and whose performance can be optimized, that is to say, is adjustable at will and remains stable over periods of time, especially when at least one of the pigments present is reactive with its own medium, the applicants in the pursuit of their researches have been able to identify and develop a pigment dispersant which renders reactive pigments such as zinc oxide, for example, particularly compatible with all emulsion polymers.
The water soluble dispersant according to this invention, which is an acrylic copolymer, is typically a copolymer of acrylic, methacrylic and itaconic acids.
Copolymers according to this invention generally contain 2.5-96% by weight but preferably 5-70% by weight of acrylic acid, from 2-85% but preferably 5-70% of methacrylic acid and 2-40% but preferably 5-35% of itaconic acid.
Unlike previous state-of-the-art solutions in which the water soluble pigment dispersant is a copolymer of at least one ethylenic acid and of at least one ethylenic ester, in this invention the water soluble dispersant is a copolymer which entirely consists of three ethylenic acids.
These acrylic copolymers are prepared according to known processes by radical copolymerization of acrylic, methacrylic and itaconic acids in the presence of either a redox polymerization system using typically organic compounds based on hydroxylamine, metabisulfite, peroxides and persalts, for example, such as hydrogen peroxide or persulfate . . . , either in the presence of initiators such as azobisdi-isobutyronitrile, whether in the presence or not of chain transfer agents such as alcohols or mercaptans . . . .
On completion of polymerization, the aqueous polymerisate solution obtained can be used as it is as an acid or can be partially or totally neutralized by at least one suitable neutralizing agent with a mono or polyvalent function.
The total or partial neutralizing agent with a monovalent function is selected from a group consisting of alkaline cations, in particular sodium and potassium, or possibly ammonium or even primary, secondary or teritary aliphatic and/or cyclical amines, such as the ethanol amines (mono, di- or tri-ethanol amine), mono and di-ethylamine, cyclohexylamine, methyl-cyclohexylamine or amino-methylpropanol . . . .
The partial or total neutralizing agent with a polyvalent function is on the other hand selected from a group consisting of divalent alkaline earth cations, in particular magnesium, manganese and calcium or even zinc, and also by trivalent cations, aluminum or even in the case of cations of higher valency such as aliphatic and/or cyclical polyamines such as ethylene diamine, diethylene triamine and phenylene diamine, for example.
The partial or toal neutralization of the acid copolymer sites can be easily obtained by the possible combinations between at least one neutralizing agent with a monovalent function and at least one neutralizing agent with a polyvalent function.
However, the aqueous polymerisate solution can also be processed by all state-of-the-art methods to eliminate its liquid phase and isolate the acrylic copolymers in the form of a fine powder which can be used in this other form as a dispersant.
The water soluble dispersant according to this invention is, as the applicants have been able to establish, a fraction of acrylic, methacrylic and itaconic acid copolymers whose specific viscosity lies in the range of 0.3-1.6, and preferably between 0.4-1.0.
The specific viscosity of copolymers according to this invention, which is indicated by the symbol "η" is determined in the following way:
A copolymer solution is prepared in the form of a sodium salt by dissolving 50 g of dry copolymer in 1,000 ml of a solution made of distilled water and 60 g of sodium chloride. Then, with a capillary viscosimeter placed in a bath thermostatically controlled at 25° C., one measures the time taken for a given volume of the above solution containing the alkaline acrylic copolymer to run off and also the time taken for the same volume of the aqueous sodium chloride solution without the above copolymers. Specific viscosity "η" can now be defined according to the following relation: ##EQU1## The capillary tube is usually selected so that the flow time of the NaCl solution without the copolymer is about 90-100 seconds, thus providing a very highly accurate measurement of specific viscosity.
This invention also concerns water-based pigment compounds comprising a liquid phase, an emulsion polymer of the second type obtained by copolymerization of hydrophobic monomers and of an anionic hydrophilic monomer, of finely powdered pigments, one of which at least is reactive with regard to its own medium, inorganic fillers, various state-of-the-art additives and finally the dispersant which is a water soluble copolymer of the type defined in the framework of this invention.
The pigments used in the preparation of water-based pigment compounds according to this invention are generally polyvalent metal compounds of which typical examples are non-reactive pigments such as titanium dioxide as well as the other pigments derived from titanium, barium sulfate, calcium carbonate, kaolin, talc, mica, silica, clays in general, ferrous oxide, carbon black, cadmium sulfide, chrome oxides but also pigments which are reactive with their medium, such as typically and preferably zinc oxide, zinc molybdate, zinc chromate, lead silico-chromate, barium metaborate, and titanium oxides surface-treated with a coating containing zinc oxide.
Water-based pigment compounds according to this invention, compared with those using prior art dispersants can be handled even when they have a high dry matter content, that is to say a low liquid phase, as well as other lengthy periods at rest, even after several months.
The liquid phase of this type of compound generally consists of water and/or a compound which can be mixed with water such as a mono or polyalcohol, for example a mono and polyglycol, ethers and esters of mono or polyalcohol or of mono or polyglycol, such as for example, ethylene glycol, diethylene glycol or propylene glycol.
The water soluble pigment dispersant is introduced into the water-based pigment compounds in proportions of 0.05-10, and preferably 0.5-5, which proportions are expressed in terms of a percentage by weight compared with the weight of pigments and fillers.
By the same token, water-based pigment compounds according to this invention may also contain, in line with known practice, other components than the pigment, dispersant and the dispersive liquid phase, which components are added to achieve specific effects. Thus, possible additives include biocides, anionic or non-ionic surfactants of the well-known type. But in addition, anti-foaming agents such as alcohols, mineral oils and silane compounds may also be added at the same time to water-based pigment compounds. Finally, thickeners can be used in water-based pigment compounds in order to modify their rheological characteristics with the aim of improving the smoothness of the film on the base, for example or to improve the stability of the pigment suspension. Thickeners of the well-known type which are used traditionally include for example methyl cellulose, hydroxyethyl cellulose, polyacrylic acid, acrylic and methacrylic copolymers as well as thickeners of the water soluble polyurethane-type which confer improved rheological properties on water-based pigment compounds.
Finally coalescing agents can also be added to water-based pigment compounds, which may consist of an organic solvent which may or may not mix with water such as, for example, ether-monobutylic ethylene glycol or even 2.2.4-trimethylpentanediol-1.3 mono-isobutyrate (Texanol manufactured by Eastman Chemical Products). In practice, water-based pigment compounds can be produced in the following known way (or in any known way) which consists of preparing under constant stirring a water-based solution of the dispersant copolymer according to this invention, to which the pigment(s) have been added. The medium which is obtained in this way, to which various additives of the types already referred to can be added (such as surfactants, thickeners, anti-foaming agents, biocides and coalescents) can undergo a grinding process using traditional techniques such as high speed dissolvers or micro-element grinders.
The amount of water soluble pigment dispersant to be employed will be selected within the range defined above. However, as any expert knows, this quantity will depend on the size, shape and type of the particles concerned.
A certain number of dispersants known previously could only be used in minimal quantities for the preparation of water-based pigment compounds, since the use of excessive amounts resulted in unstable dispersion and even in pigment flocculation. In the case of the water soluble dispersant according to this invention, excellent reactive pigment dispersion can be obtained compared with state-of-the-art products; this is all the more true when non-reactive pigments and fillers are concerned. This means also confers on water-based pigment compounds excellent stability over periods of time, which is demonstrated by their sustained rheological characteristics even during prolonged storage.
The familiar method of demonstrating the excellent dispersive characteristics of copolymers according to this invention and especially their ability to be employed in water-based pigment compounds where the pigments are partially or entirely reactive consists of using zinc oxide as the reactive pigment since this substance generally causes real stability problems when it is used in compounds together with an emulsion polymer of the second type as a binder. For example, paint prepared with this reactive pigment dispersed by means of one of the previously known substances, will display poor stability characteristics over periods of time. In point of fact, it is well-known that zinc oxide will partially dissolve and react with the emulsion polymer (binder) and will cause rapid degradation of the rheological characteristics of such a paint, despite the presence of a dispersant.
On the other hand, a paint prepared with the same reactive pigment using a dispersant according to the invention and where an emulsion polymer of the second type is employed, displays excellent stability over periods of time since the effectiveness of this substance can be demonstrated by the fact that the print will maintain its viscosity even after six months' aging at ambient temperature and/or one month at 60° C.
Thus, the instability of a water-based pigment compound or even the ineffectiveness of reactive pigment dispersants, such as zinc oxide, with respect to emulsion polymers of the second type, is frequently demonstrated by a sharp rise of viscosity during storage and even by the gelification or solidification of the compound itself.
It will thus be appreciated that the principal property of the dispersant according to this invention, lies in the fact that when it is employed in water-based pigment compounds, no sharp rise in viscosity is observed, nor does the product solidify during lengthy storage at ambient temperatures or during shorter term exposure to higher temperatures, when a reactive type of pigment is used.
By the same token, with a view to using a pigment paste to color an emulsion paint (which the specialist still refers to as the "tint base") which may wholly or partially contain one and/or the other reactive pigment such as zinc oxide, it is preferable to employ the dispersant according to this invention for the preparation of this pigment paste and/or in the above-mentioned tint base to ensure the stability over a period of time of the water-based pigment compound resulting from the mixing of these two components.
The scope and the interesting features of this invention will be better appreciated with the help of the following examples:
This example illustrates the use of some typical earlier state-of-the-art water-based pigment compounds, comprising among other constituents zinc oxide as a reactive pigment, an emulsion polymer or binder belonging to both of the categories referred to above and the sodium salt of a homopolymer of methacrylic acid which is a dispersant of a type formerly in common use.
For this purpose, paint was prepared according to the following method: the following constituents, expressed in parts by weight, were added one after another in a suitable two liter container, fitted with a so-called "shear-type turbine" stirring device rotating at about 1,000 rpm (this is a Cowles-type dissolver with which specialists are familiar):
______________________________________
(a) water 160
(b) hydroxyethyl cellulose as a thickener
2
(Natrosol 250 HR marketed by Hercules Inc.)
(c) a dispersant containing 30% of active constituent
8
(the sodium salt of a homopolymer of methacrylic
acid according to a Canadian patent 655,884 based on
earlier state-of-the-art)
(d) biocide additive 2
(Mergal K6N marketed by Riedel de Haen)
(e) anti-foaming additive 1.5
(BYK 073 marketed by Byk Chemie)
(f) reactive pigment: zinc oxide 40
(Neige A marketed by Vieille Montagne)
(g) non-reactive pigment 130
(RL 68 marketed by Thann et Mulhouse)
(h) fillers:
(h1) calcium carbonate 220
(BLP2 marketed by Omya Inc.)
(h2) talc 30
(20 MO marketed by the Societe des Talcs de
Luzenac)
(i) monoethylene glycol 10
(j) emulsion polymer: binder expressed in parts of dry
162.5
matter
(k) coalescing solvent 15
(Texanol marketed by Eastman Chemical Prdts)
(l) water to make up a total of 993.5 parts by weight
______________________________________
Three mixtures were prepared in this way using different emulsion polymers as binders which are submitted to an accelerated aging test in an oven at 60° C. for one month and to a storage test at ambient temperature for six months; at the end of this period viscosity was measured using a Brookfield (RVT)-type viscosimeter at 10 rpm. All the results are summarized in Table I below:
TABLE I
______________________________________
VISCOSITY
AFTER
VIS- VISCOSITY 6 MONTHS
COSITY AFTER STORAGE
AFTER 1 MONTH AT AMBIENT
EMULSION 24 H IN AT 60° C.
TEMPERATURE
POLYMER CENTI- IN CENTI- IN CENTI-
(BINDER) POISES POISES POISES
______________________________________
Formulation 1
5 800 5 500 6 000
Type 1 copolymer
of acrylic or
methacrylic esters
with protective
colloid. (Primal
AC 507 marketed
by Rohm & Haas)
Formulation 2
5 200 5 500 5 400
Type 1 copolymer
of acrylic or
methacrylic esters
with protective
colloid (Primal
AC 388 marketed
by Rohm & Haas)
Formulation 3
8 500 Solid- Solid-
Type 2 styrene ification ification
and acrylic ester after 1 after two
copolymer w/o week months
protective colloid
______________________________________
The above results show that in the case of emulsion polymers (type 1 binders) with a protective colloid, the rheological characteristics of water-based pigment compounds remain stable over periods of time, whereas in the case of emulsion polymers (type 2 binders) without protective colloids, the rheological characteristics of water-based pigment compounds degrade extremely rapidly (solidification).
This example shows three typical water-based pigment compounds according to earlier state-of-the-art, comprising among their various constituents zinc oxide as a reactive pigment, an emulsion polymer (binder) belonging to the type 2 classification referred to above without protective colloids, and various dispersants used in earlier state-of-the-art techniques.
For this purpose, a semigloss paint was prepared according to the same method as used in Example 1 above, by adding the following components in turn, the quantities being expressed in parts by weight:
______________________________________
(a) water 50
(b) monopropylene glycol 40
(c) a dispersant expressed in terms of active matter
4.6
(defined in Table II below)
(d) biocide additive 3
(Mergal K6N marketed by Riedel de Haen)
(e) anti-foaming additive 2
(Nopco NDW marketed by Diamond-Shamrock Inc.)
(f) reactive pigment: zinc oxide 40
(Neige A marketed by Vieille Montagne)
(g) non-reactive pigment: titanium dioxide
190
(RHD2 marketed by Tioxide Inc.)
(h) filler: calcium carbonate 120
(Hydrocarb L marketed by Omya Inc.)
(i) coalescing solvent (butyl diglycol)
20
(j) emulsion polymer (binder) 440
(Acronal 290 D, a type 2 polymer without protective
colloids, a styrene and acrylic ester copolymer
marketed by BASF)
(k) thickener: water soluble polyurethane
51
(in a 10% by weight solution - BR 100 marketed by
Coatex)
(l) water 40
______________________________________
Three mixtures (4, 5, 6) were prepared in this way, each of which contained a specific earlier state-of-the-art dispersant and the mixtures were submitted to the same aging tests as in Example 1 above.
The results of all these tests are shown in Table II below:
TABLE II
______________________________________
VIS- VISCOSITY
COSITY AFTER 6
VIS- AFTER MONTHS
COSITY 1 MONTH STORAGE
AFTER AT 60°
AT AMBIENT
24 H. IN C. IN TEMPERATURE
CENTI- CENTI- IN CENTI-
DISPERSANT POISES POISES POISES
______________________________________
FORMULATION 4
3 000 Solid- Solid-
Acrylic acid ification ification
butyl acrylate after 1
copolymer accord- week
ing to U.S. Pat. No. 3840487
FORMULATION 5
10 000 Solid- Solid-
Tamol SG 1 ification ification
marketed by Rohm after 1
& Haas week
FORMULATION 6
2 400 Solid- Solid-
Acrylic acid (30%) ification ification
methacrylic acid after two
(30%) itaconic acid weeks
(11%) and butyl
acrylate copolymer
______________________________________
These results show that when an emulsion polymer (binder) of the second type without protective colloids, of a type which is being more and more widely used, is associated with a reactive pigment such as zinc oxide together with an earlier type of dispersant, the result will be rapid solidification of the water-based pigment compounds containing these substances.
This example shows a means of preparing the dispersant according to this invention.
For this purpose, a 1,000 ml vessel was fitted with a mechanical stirrer, a vertical condensor, a means of heating and three dosing pumps.
200 g of deionized water and 0.3 g of copper acetate were placed in the vessel and heated to a reflux temperature before simultaneously adding over a period of two hours the following solutions 1-3 with the dosing pumps:
______________________________________
Solution 1:
deionized water 147.0 g
methacrylic acid 99.2 g
acrylic acid 108.5 g
itaconic acid 12.1 g
Solution 2:
deionized water 42.5 g
hydrogen peroxide (130 vols)
30.0 g
Solution 3:
deionized water 60.0 g
sodium metabisulfite
2.0 g
______________________________________
Solutions 2 and 3 comprise the redox polymerization system.
After adding the above components, the mixtures were maintained at their reflux temperature for one hour. The resulting polymer was neutralized down to a pH of 8.5 with sodium hydroxide, resulting in a solution containing 35% active matter by weight.
This example illustrates the preparation, according to the method described in Example 3, of dispersants based either on earlier state-of-the-art or according to this invention, and other incorporation in water-based pigment compounds comprising among their various constituents zinc oxide as a reactive pigment, a type 2 emulsion polymer (or binder) referred to above, that is to say without protective colloids and various dispersants from earlier state-of-the-art practice (formulations 7-10) as well as dispersants according to this invention (formulations 11-16).
For the preparation of dispersants, both of the earlier state-of-the-art type as well as according to this invention, the three water-based solutions referred to in Example 3 were used, the first solution containing monomers and solutions 2 and 3 constituting the redox polymerization system.
On completion of polymerization and neutralization with sodium hydroxide down to a pH of 8.5, a copolymer solution was obtained whose specific viscosity was measured.
Four polymers were also prepared based on earlier state-of-the-art (refs. A, B, C, and D) as well as six copolymers according to this invention (refs. E, F, G, H, I and J) for which the composition of the monomer and/or redox polymerization system was varied.
A paint was then prepared (a water-based pigment compound) according to the same method as Example 1, by adding in turn the following constituents expressed in parts by weight:
______________________________________
(a) water 160
(b) thickener: hydroxyethyl cellulose
2
(Natrosol 250 HR marketed by Hercules Inc.)
(c) a dispersant expressed as dry matter
3
(d) biocide additive 1
(Mergal K6N marketed by Riedel de Haen)
(e) anti-foaming additive 1.5
(BYK 073 marketed by Byk Chemie)
(f) reactive pigment: zinc oxide 40
(Neige A marketed by Vieille Montagne)
(g) non-reactive pigment: titanium oxide
130
(RL 68 marketed by Thann et Mulhouse)
(h) fillers:
(h1) calcium carbonate 140
(Durcal 5 marketed by Omya Inc., mean diameter
5 microns)
(h2) calcium carbonate 80
(Hydrocarb marketed by Omya Inc., mean diameter
1 micron)
(i) monoethylene glycol 10
(j) type 2 emulsion polymer without protective colloid
325
containing 50% of dry matter (binder)
(Rhodopas DS 910 marketed by Rhone-Poulenc)
(k) coalescent solvent 0.5
(Texanol marketed by Eastman Chemical Products)
(l) water to make a total of 993 parts by weight
______________________________________
Four formulations were prepared in this way (7-11) using various dispersants (A, B, C, D and E) based on previous state-of-the-art and six formulations (12-17) were prepared using various dispersants (F, G, H, I, J and K) according to this invention (all the formulations were submitted to accelerated aging tests at 60° C. in an autoclave for a period of one month and to a storage test at ambient temperature lasting six months, at the end of which periods Brookfield viscosity was measured as in Example 1.
All the results concerning the preparation of earlier state-of-the-art dispersants A-D as well as the results concerning water-based pigment compounds in which these dispersants were used (formulations 7-10) are summarized in Table III below:
TABLE III
______________________________________
EARLIER STATE OF THE
PERCENTAGE ART DISPERSANT
BY WEIGHT A B C D E
______________________________________
Acrylic acid 0 100 0 0 55
Methacrylic 100 0 70 55 0
acid
Itaconic 0 0 0 15 15
acid
Butyl meth- 0 0 30 30 30
acrylate
Specific visc.
0.90 0.75 0.71 0.79 0.84
Formulations 7 8 9 10 11
(Water-based
pigment com-
pounds)
Viscosity in 15000 16000 12000 13000 15000
centipoises
after 24 hrs.
Viscosity in Solid- Solid- Solid-
Solid-
Solid-
centi- ifica- ifica- ifica-
ifica-
ifica-
poises after tion tion tion tion tion
1 month at 60° C.
Viscosity in Solid- Solid-
Solid-
Solid-
centipoises ifica- ifica-
ifica-
ifica-
after 6 months tion tion tion tion
storage at amb-
ient temp.
______________________________________
All the results concerning the preparation of dispersants according to the invention (F, G, H, I, J and K) as well the results concerning water-based pigment compounds incorporating these dispersants (formulations 12-17) are summarized in Table IV below:
TABLE IV
______________________________________
PERCENT DISPERSANTS ACCORDING
AGE BY TO THE INVENTION
WEIGHT F G H I J K
______________________________________
Acrylic acid
49.4 44.5 41.8 64.6 44.5 44.5
Methacrylic
45.1 40.50 38.3 5.2 40.5 40.5
acid
Itaconic 5.5 15.00 19.9 30.2 15.0 15.0
acid
Specific visc.
0.54 0.65 0.60 0.50 0.90 0.42
Formulations
12 13 14 15 16 17
(Water-based
pigment com-
pounds)
Viscosity in
6200 7000 8200 6000 7400 6800
centipoises
after 24 hrs.
Viscosity in
6600 8000 10800 10800 13400 10400
centipoises
after 1 month
at 60° C.
Viscosity in
12400 10000 13000 17200 16000 23000
centipoises
after 6
months stor-
age at amb-
ient temp.
______________________________________
A comparison of Tables III and IV shows the effectiveness of dispersants according to this invention, since the rheological characteristics of water-based pigment compounds containing these dispersants do not alter or alter only very slightly over periods of time, whereas the rheological characteristics of water-based pigment compounds containing earlier state-of-the-art dispersants are subject to violent changes, going as far as solidification.
The purpose of this example is to show that the water soluble dispersant according to this invention is a fraction of acrylic, methacrylic and itaconic acid copolymers whose specific viscosity is selected between 0.3-1.6 and preferably between 0.4-1.0.
For this purpose, dispersants according to this invention were prepared using the method described in Example 3, varying the quantity of the redox system employed.
Then, these dispersants were incorporated in water-based pigment compounds identical to the compound in Example 4, that is to say containing zinc oxide as a reactive pigment and an emulsion polymer without a protective colloid (type 2).
Five polymers (refs. J, K, L, M and N) were prepared in this way and were incorporated in five water-based pigment compounds (formulations 16, 17, 18, 19 and 20).
All these formulations were submitted to the same aging tests as in Example 4.
The results concerning the preparation of all dispersants according to this invention as well as those concerning water-based pigment compounds in which these dispersants were incorporated, are summarized in Table V below:
TABLE V
______________________________________
DISPERSANTS ACCORDING
PERCENTAGE TO THE INVENTION
BY WEIGHT J K L M N
______________________________________
Acrylic acid
44.5 44.5 44.4 44.5 44.5
Methacrylic 40.5 40.5 40.5 40.5 40.5
acid
Itaconic 15.0 15.0 15.0 15.0 15.0
acid
Specific visc.
0.90 0.42 0.31 1.53 1.70
Formulations
16 17 18 19 20
(Water-based
pigment com-
pounds)
Viscosity in
7400 6800 8200 9600 12500
centipoises
after 24 hrs.
Viscosity in
13400 10400 18500 22000 36200
centi-
poises after
1 month at 60° C.
Viscosity in
16000 23000 55000 48000 Solid-
centipoises ification
after 6 months
storage at amb-
ient temp.
______________________________________
It can thus be seen that outside the limits of specific viscosity established by the applicants, the dispersant according to the invention very rapidly loses its effectiveness, as shown by the viscosity changes affecting water-based pigment compounds containing these dispersants.
The purpose of this example is to verify that the dispersant according to this invention must be a copolymer formed from three acrylic, methacrylic and itaconic acid monomers and that copolymerization of these monomers pair by pair results in dispersants whose effectiveness is reduced when they are incorporated in water-based pigment compounds containing a reactive pigment such as zinc oxide and an emulsion polymer (type 2) without a protective colloid.
For this purpose, dispersants obtained by copolymerization of two monomers selected among the three referred to above, were prepared according to the method used in Example 3 (refs. O, P and Q).
These dispersants were then incorporated in water-based pigment compounds identical to those in Example 4, that is to say containing a reactive pigment (zinc oxide) and an emulsion polymer without a protective colloid (type 2).
The effectiveness of these three dispersants was compared with that of the dispersant (G) according to the invention (Table IV) incorporated in the same water-based pigment compound as that described in Example 4.
All the results concerning the preparation of these dispersants (refs. O, P and Q) as well as the preparation of the dispersant according to the invention (ref. G) together with the results concerning water-based pigment compounds (formulations 18-23) incorporating these dispersants, have been summarized in Table VI below:
TABLE VI
______________________________________
PERCENTAGE DISPERSANTS
BY WEIGHT O P Q G (Invention)
______________________________________
Acrylic acid
0. 85.0 50.0 44.5
Methacrylic 85.0 0. 50.0 40.5
acid
Itaconic 15.0 15.0 0 15.0
acid
Specific visc.
0.54 0.67 0.70 0.65
Formulations
18 19 20 13
(Water-based
pigment com-
pounds)
Viscosity in
8200 11000 10500 7000
centipoises
after 24 hrs.
Viscosity in
10200 28000 25000 8000
centipoises
after 1 month
at 60° C.
Viscosity in
53000 Solid- 48000 10000
centipoises ification
after 6 months
storage at amb-
ient temp.
______________________________________
The results obtained confirm that it is absolutely essential that the dispersant according to this invention, be an acrylic, methacrylic and itaconic acid copolymer.
Claims (20)
1. A process for the preparation of an aqueous pigment composition comprising:
forming an aqueous dispersion containing a liquid emulsion of a polymer free of protective colloids and having a high density of anionic groups, of pigments containing metal ions, with a water-soluble dispersant which is a copolymer of acrylic acid, methacrylic acid and itaconic acid, the said dispersant having reactive carboxylate groups which can bond with the metal ions of said pigment while inhibiting their reaction with the emulsion polymer and said dispersant conferring on said aqueous pigment composition definable rheological characteristics which can be established beforehand and which remain stable over a period of time.
2. The process of claim 1, wherein said copolymer comprises from 2.5-96% by weight of acrylic acid, 2-95% by weight of methacrylic acid and 2-40% by weight of itaconic acid.
3. The process of claim 2, wherein said copolymer comprises from 5-70% by weight of acrylic acid, 5-70% by weight of methacrylic acid and 5-35% by weight of itaconic acid.
4. The process of claim 1, wherein the copolymers which constitute the said dispersant are partially neutralized.
5. The process of claim 1, wherein the copolymers which constitute the said dispersant are wholly neutralized.
6. The process of claim 1, wherein said copolymer is neutralized by at least one neutralizing agent which is a monovalent compound or a polyvalent compound.
7. The process of claim 6, wherein said copolymer is neutralized by at least one monovalent compound and at least one polyvalent compound.
8. The process of claim 6, wherein said monovalent neutralizing compound is an alkali compound.
9. The process of claim 8, wherein the alkali component of the neutralizing compound is selected from the group consisting of sodium, potassium, ammonium and an ion of a primary, secondary or tertiary aliphatic and/or cyclic amine.
10. The process of claim 9, wherein said amine ion is an ion of ethanolamine, monoethylamine, diethylamine, cyclohexylamine, methyl-cyclohexylamine or aminomethylpropanol.
11. The process of claim 6, wherein said polyvalent neutralizing compound is an alkaline earth metal compound, a trivalent metal compound or a polyvalent ion of an aliphatic and/or cyclic polyamine.
12. The process of claim 11, wherein said alkaline earth metal is calcium, magnesium, manganese or zinc, said trivalent metal is aluminum, and said polyamine is ethylenediamine, diethylene triamine or phenylene diamine.
13. The process of claim 1, wherein said copolymer of said dispersant has a specific viscosity of 0.3-1.6.
14. The process of claim 13, wherein said specific viscosity ranges from 0.4-1.0.
15. An aqueous pigment composition comprising:
an aqueous dispersion containing a liquid emulsion of a polymer free of protective colloids and having a high density of anionic groups, of pigments containing metal ions, with a water-soluble dispersant which is a copolymer of acrylic acid, methacrylic acid and itaconic acid, the said dispersant having reactive carboxylate groups which can bond with the metal ions of said pigment while inhibiting their reaction with the emulsion polymer and said dispersant conferring on said aqueous pigment composition definable rheological characteristics which can be established beforehand and which remain stable over a period of time.
16. The composition of claim 15, wherein the copolymer dispersant is present in an amount ranging from 0.05-10% by weight based on the amount of filler and pigment in the composition.
17. The composition of claim 16, wherein the amount of said copolymer dispersant ranges from 0.5-5% by weight.
18. The composition of claim 15, wherein the aqueous phase of said dispersion further comprises an organic solvent which can be mixed with water and which is a compound selected from the group consisting of a mono- or polyalcohol, a mono- or polyglycol, an ether or ester of said mono- or polyalcohol and an ether or ester of said mono- or polyglycol.
19. The composition of claim 15, wherein said pigment is a reactive pigment selected from the group consisting of zinc oxide, zinc molybdate, zinc chromate, lead silico-chromate, barium metaborate and titanium oxides surface treated with zinc oxide.
20. The composition of claim 15, which further comprises at least one constituent selected from the group consisting of biocides, anionic or non-ionic surfactants, anti-foaming agents, thickeners and coalescing agents.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8418579A FR2574086B1 (en) | 1984-12-03 | 1984-12-03 | WATER-SOLUBLE DISPERSING AGENT FOR PIGMENTED AQUEOUS COMPOSITIONS |
| FR8418579 | 1984-12-03 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06739704 Continuation | 1985-05-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4687789A true US4687789A (en) | 1987-08-18 |
Family
ID=9310277
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/837,575 Expired - Fee Related US4687789A (en) | 1984-12-03 | 1986-03-04 | Water soluble dispersant for water-based pigment compounds comprising a terpolymer of acrylic acid methacrylic acid and itaconic acid |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4687789A (en) |
| JP (1) | JPS61148271A (en) |
| BE (1) | BE903772A (en) |
| CA (1) | CA1256636A (en) |
| CH (1) | CH667103A5 (en) |
| DE (1) | DE3542308A1 (en) |
| ES (2) | ES8706784A1 (en) |
| FR (1) | FR2574086B1 (en) |
| GB (1) | GB2168062B (en) |
| GR (1) | GR852889B (en) |
| IT (1) | IT1201501B (en) |
| NL (1) | NL8503327A (en) |
| SE (1) | SE465779B (en) |
Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5116407A (en) * | 1988-10-13 | 1992-05-26 | Courtaulds Coatings Limited | Antifouling coatings |
| US5120359A (en) * | 1988-02-26 | 1992-06-09 | Sakura Color Products Corporation | Erasable ink compositions |
| US5236493A (en) * | 1988-10-13 | 1993-08-17 | Courtaulds Coatings (Holdings) Limited | Antifouling coating |
| US5275650A (en) * | 1987-10-23 | 1994-01-04 | Coatex S.A. | Agent for grinding lime to augment its reactivity |
| US5276075A (en) * | 1991-10-30 | 1994-01-04 | Binney & Smith Inc. | Washable acrylic paint |
| US5284894A (en) * | 1990-02-22 | 1994-02-08 | Basf Corporation | Low-foaming latexes for use in printing ink formulations |
| US5296531A (en) * | 1991-12-20 | 1994-03-22 | Basf Aktiengesellschaft | Pigment preparations |
| EP0676422A1 (en) * | 1994-04-05 | 1995-10-11 | Rohm And Haas Company | Aqueous process for preparing low molecular weight polymers |
| US5492614A (en) * | 1994-05-25 | 1996-02-20 | Ppg Industries, Inc. | Method of electrodeposition using an electrocoating composition containing a low volatile organic content pigment grind composition |
| US5530043A (en) * | 1994-05-25 | 1996-06-25 | Ppg Industries, Inc. | Low volatile organic content pigment grind composition |
| US5872162A (en) * | 1993-06-04 | 1999-02-16 | The Gillette Company | Correction fluid for water-fast inks |
| US5877234A (en) * | 1994-10-31 | 1999-03-02 | The Gillette Company | Water-based correction fluid |
| US5891237A (en) * | 1997-10-08 | 1999-04-06 | Millennium Inorganic Chemicals, Ltd. | Production of free flowing spheres using partially neutralized fatty acid |
| US5922400A (en) * | 1997-01-09 | 1999-07-13 | The Gillette Company | Correction fluid |
| US6083618A (en) * | 1997-06-25 | 2000-07-04 | The Gillette Company | Correction fluids comprising composite polymeric particles |
| US6576336B1 (en) * | 1998-09-11 | 2003-06-10 | Unitech Corporation, Llc | Electrically conductive and electromagnetic radiation absorptive coating compositions and the like |
| US20040028859A1 (en) * | 1998-09-11 | 2004-02-12 | Legrande Wayne B. | Electrically conductive and electromagnetic radiation absorptive coating compositions and the like |
| US20040162383A1 (en) * | 2002-02-25 | 2004-08-19 | Morrison Jr William Harvey | Unfinished rutile titanium dioxide slurry for paints and paper coatings |
| US20050282946A1 (en) * | 2004-06-21 | 2005-12-22 | Tyau-Jeen Lin | Titanium dioxide slurries for ink applications |
| US20060140987A1 (en) * | 2004-11-08 | 2006-06-29 | Reeve Paul Francis D | Aqueous compositions with poorly water soluble compounds |
| US20080166565A1 (en) * | 2003-01-28 | 2008-07-10 | Nobuyuki Ikeguchi | Lubricant sheet for drilling and method of drilling |
| CN106634212A (en) * | 2015-10-28 | 2017-05-10 | 株式会社理光 | Ink, method of manufacturing ink, and ink cartridge |
| US11352511B2 (en) * | 2017-05-12 | 2022-06-07 | Toyo Ink Sc Holdings Co., Ltd. | Dispersant, dispersant composition, dispersion composition for batteries, electrode and battery |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0260577A1 (en) * | 1986-09-11 | 1988-03-23 | The B.F. Goodrich Company | Ash-free multivalent cationstable dispersants for inorganic powders |
| US4952617A (en) * | 1987-11-06 | 1990-08-28 | Columbian Chemicals Company | Dispersion of pigments in resins and coatings systems |
| US5431846A (en) * | 1993-05-20 | 1995-07-11 | Lever Brothers Company, Division Of Conopco, Inc. | Copolymers and detergent compositions containing them |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0125519A1 (en) * | 1983-04-20 | 1984-11-21 | Société COATEX, Société Anonyme | Water soluble complexing agent for metallic cations composed of acrylic terpolymers with a high complexing power |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4243430A (en) * | 1977-09-21 | 1981-01-06 | Rohm And Haas Company | Pigment dispersant for aqueous paints |
| DE3233776A1 (en) * | 1982-09-11 | 1984-03-15 | Basf Ag, 6700 Ludwigshafen | METHOD FOR PRODUCING COPOLYMERISATES FROM MONOETHYLENICALLY UNSATURATED MONO- AND DICARBONIC ACIDS |
| JPH0653870B2 (en) * | 1983-04-15 | 1994-07-20 | サンノプコ株式会社 | Light calcium carbonate dispersant |
-
1984
- 1984-12-03 FR FR8418579A patent/FR2574086B1/en not_active Expired
-
1985
- 1985-11-25 CH CH5015/85A patent/CH667103A5/en not_active IP Right Cessation
- 1985-11-25 SE SE8505567A patent/SE465779B/en not_active IP Right Cessation
- 1985-11-25 CA CA000496111A patent/CA1256636A/en not_active Expired
- 1985-11-29 DE DE19853542308 patent/DE3542308A1/en not_active Withdrawn
- 1985-12-02 NL NL8503327A patent/NL8503327A/en not_active Application Discontinuation
- 1985-12-02 GB GB8529663A patent/GB2168062B/en not_active Expired
- 1985-12-02 BE BE0/215950A patent/BE903772A/en not_active IP Right Cessation
- 1985-12-02 IT IT23055/85A patent/IT1201501B/en active
- 1985-12-02 GR GR852889A patent/GR852889B/el unknown
- 1985-12-03 ES ES549513A patent/ES8706784A1/en not_active Expired
- 1985-12-03 JP JP60272359A patent/JPS61148271A/en active Pending
-
1986
- 1986-03-04 US US06/837,575 patent/US4687789A/en not_active Expired - Fee Related
-
1987
- 1987-02-13 ES ES557388A patent/ES8900096A1/en not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0125519A1 (en) * | 1983-04-20 | 1984-11-21 | Société COATEX, Société Anonyme | Water soluble complexing agent for metallic cations composed of acrylic terpolymers with a high complexing power |
Non-Patent Citations (2)
| Title |
|---|
| Derwent Abstract 84 289832/47, Soc. Coatex EP 125519. * |
| Derwent Abstract 84-289832/47, Soc. Coatex EP-125519. |
Cited By (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5275650A (en) * | 1987-10-23 | 1994-01-04 | Coatex S.A. | Agent for grinding lime to augment its reactivity |
| US5120359A (en) * | 1988-02-26 | 1992-06-09 | Sakura Color Products Corporation | Erasable ink compositions |
| US5116407A (en) * | 1988-10-13 | 1992-05-26 | Courtaulds Coatings Limited | Antifouling coatings |
| US5236493A (en) * | 1988-10-13 | 1993-08-17 | Courtaulds Coatings (Holdings) Limited | Antifouling coating |
| US5284894A (en) * | 1990-02-22 | 1994-02-08 | Basf Corporation | Low-foaming latexes for use in printing ink formulations |
| US5276075A (en) * | 1991-10-30 | 1994-01-04 | Binney & Smith Inc. | Washable acrylic paint |
| US5296531A (en) * | 1991-12-20 | 1994-03-22 | Basf Aktiengesellschaft | Pigment preparations |
| US5872162A (en) * | 1993-06-04 | 1999-02-16 | The Gillette Company | Correction fluid for water-fast inks |
| EP0676422A1 (en) * | 1994-04-05 | 1995-10-11 | Rohm And Haas Company | Aqueous process for preparing low molecular weight polymers |
| US5601723A (en) * | 1994-04-05 | 1997-02-11 | Rohm And Haas Company | Method of inhibiting scale and corrosion in aqueous systems using low molecular weight polymers |
| US6335404B1 (en) | 1994-04-05 | 2002-01-01 | Rohm And Haas Company | Aqueous process for preparing aqueous weight carboxyl containing polymers |
| US5492614A (en) * | 1994-05-25 | 1996-02-20 | Ppg Industries, Inc. | Method of electrodeposition using an electrocoating composition containing a low volatile organic content pigment grind composition |
| US5530043A (en) * | 1994-05-25 | 1996-06-25 | Ppg Industries, Inc. | Low volatile organic content pigment grind composition |
| US5877234A (en) * | 1994-10-31 | 1999-03-02 | The Gillette Company | Water-based correction fluid |
| US6025413A (en) * | 1994-10-31 | 2000-02-15 | The Gillette Company | Water-based correction fluid |
| US5922400A (en) * | 1997-01-09 | 1999-07-13 | The Gillette Company | Correction fluid |
| US6083618A (en) * | 1997-06-25 | 2000-07-04 | The Gillette Company | Correction fluids comprising composite polymeric particles |
| US5891237A (en) * | 1997-10-08 | 1999-04-06 | Millennium Inorganic Chemicals, Ltd. | Production of free flowing spheres using partially neutralized fatty acid |
| US6576336B1 (en) * | 1998-09-11 | 2003-06-10 | Unitech Corporation, Llc | Electrically conductive and electromagnetic radiation absorptive coating compositions and the like |
| US20040028859A1 (en) * | 1998-09-11 | 2004-02-12 | Legrande Wayne B. | Electrically conductive and electromagnetic radiation absorptive coating compositions and the like |
| US20040162383A1 (en) * | 2002-02-25 | 2004-08-19 | Morrison Jr William Harvey | Unfinished rutile titanium dioxide slurry for paints and paper coatings |
| US7186770B2 (en) | 2002-02-25 | 2007-03-06 | E. I. Du Pont De Nemours And Company | Unfinished rutile titanium dioxide slurry for paints and paper coatings |
| US20080166565A1 (en) * | 2003-01-28 | 2008-07-10 | Nobuyuki Ikeguchi | Lubricant sheet for drilling and method of drilling |
| US9211592B2 (en) * | 2003-01-28 | 2015-12-15 | Mitsubishi Gas Chemical Company, Inc. | Lubricant sheet for drilling and method of drilling |
| US20080255281A1 (en) * | 2004-06-21 | 2008-10-16 | Tyau-Jeen Lin | Titanium dioxide slurries for ink applications |
| US20050282946A1 (en) * | 2004-06-21 | 2005-12-22 | Tyau-Jeen Lin | Titanium dioxide slurries for ink applications |
| US20060140987A1 (en) * | 2004-11-08 | 2006-06-29 | Reeve Paul Francis D | Aqueous compositions with poorly water soluble compounds |
| CN106634212A (en) * | 2015-10-28 | 2017-05-10 | 株式会社理光 | Ink, method of manufacturing ink, and ink cartridge |
| US10844235B2 (en) | 2015-10-28 | 2020-11-24 | Ricoh Company, Ltd. | Ink, method of manufacturing ink, and ink cartridge |
| US11352511B2 (en) * | 2017-05-12 | 2022-06-07 | Toyo Ink Sc Holdings Co., Ltd. | Dispersant, dispersant composition, dispersion composition for batteries, electrode and battery |
Also Published As
| Publication number | Publication date |
|---|---|
| ES8706784A1 (en) | 1987-07-01 |
| ES549513A0 (en) | 1987-07-01 |
| ES8900096A1 (en) | 1988-12-01 |
| GB2168062A (en) | 1986-06-11 |
| FR2574086A1 (en) | 1986-06-06 |
| DE3542308A1 (en) | 1986-06-19 |
| GR852889B (en) | 1986-04-03 |
| CH667103A5 (en) | 1988-09-15 |
| IT1201501B (en) | 1989-02-02 |
| JPS61148271A (en) | 1986-07-05 |
| SE8505567D0 (en) | 1985-11-25 |
| FR2574086B1 (en) | 1987-07-17 |
| SE465779B (en) | 1991-10-28 |
| SE8505567L (en) | 1986-06-04 |
| GB8529663D0 (en) | 1986-01-08 |
| ES557388A0 (en) | 1988-12-01 |
| BE903772A (en) | 1986-04-01 |
| GB2168062B (en) | 1989-08-02 |
| NL8503327A (en) | 1986-07-01 |
| IT8523055A0 (en) | 1985-12-02 |
| CA1256636A (en) | 1989-06-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: COATEX S.A., 35 COURS ARISTIDE BRIAND, 69300 CALUI Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:GONNET, OLIVIER;ROUSSET, JACKY;REEL/FRAME:004721/0932 Effective date: 19850701 |
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Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
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| FPAY | Fee payment |
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| LAPS | Lapse for failure to pay maintenance fees | ||
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Effective date: 19950823 |
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| STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |